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Organic electroluminescent device

an electroluminescent device and organic technology, applied in the field of organic electroluminescent devices, can solve the problems of deterioration of the device, inability to achieve improvement in luminous efficiency, and material degradation

Active Publication Date: 2017-11-30
HODOGOYA CHEMICAL CO LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides an organic EL device with excellent hole injection and transport performance, low driving voltage, and high luminous efficiency. This is achieved by selecting a specific arylamine compound with a specific structure as the material of the hole injection layer and p-doping the compound with an electron acceptor to efficiently inject and transport holes into a hole transport layer from an electrode. Furthermore, without p-doping the compound as the material of the hole transport layer, an organic EL device with low driving voltage, high luminous efficiency, and a long lifetime can be realized by refining carrier balance. The present invention also improves durability while maintaining low driving voltage of conventional organic EL devices.

Problems solved by technology

The materials with low heat resistance cause thermal decomposition even at a low temperature by heat generated during the drive of the device, which leads to the deterioration of the materials.
The materials with low amorphousness cause crystallization of a thin film even in a short time and lead to the deterioration of the device.
However, since the compound is insufficient in terms of electron blocking performance, some of the electrons pass through the light emitting layer, and improvements in luminous efficiency cannot be expected.
However, while the devices using these compounds for the hole injection layer or the hole transport layer have been improved in lower driving voltage, heat resistance, luminous efficiency and the like, the improvements are still insufficient.

Method used

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  • Organic electroluminescent device
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Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of N,N-bis(biphenyl-4-yl)-N-(6-phenylbiphenyl-3-yl)amine (Compound 1-2)

[0221]N,N-bis(biphenyl-4-yl)-N-(6-bromobiphenyl-3-yl)amine (11.8 g), toluene (94 mL), phenylboronic acid (2.7 g), and an aqueous solution obtained by previously dissolving potassium carbonate (5.9 g) in water (36 mL) were added into a nitrogen-substituted reaction vessel and aerated with nitrogen gas under ultrasonic irradiation for 30 minutes. Tetrakistriphenylphosphine palladium (0.74 g) was added thereto, and the resulting mixture was heated and stirred at 72° C. for 18 hours. After the mixture was cooled to a room temperature, an organic layer was collected by liquid separation. The organic layer was washed with water, and washed with a saturated salt solution sequentially, and then dried over anhydrous magnesium sulfate and concentrated to obtain a crude product. Subsequently, the crude product was purified using column chromatography, whereby a white powder of N,N-bis(biphenyl-4-yl)-N-(6-phenylbip...

example 2

Synthesis of N,N-bis(biphenyl-4-yl)-N-{6-(naphthyl-1-yl)biphenyl-3-yl}amine (Compound 1-3)

[0225]The reaction was carried out under the same conditions as those of Example 1, except that phenylboronic acid was replaced with 1-naphthylboronic acid, whereby a white powder of N,N-bis(biphenyl-4-yl)-N-{6-(naphthyl-1-yl)biphenyl-3-yl}amine (Compound 1-3, 9.2 g, yield: 61%) was obtained.

[0226]The structure of the obtained white powder was identified by NMR.

[0227]1H-NMR (CDCl3) detected 33 hydrogen signals, as follows.

[0228]δ (ppm)=7.84-7.87 (3H), 7.67-83 (6H), 7.26-7.64 (18H) 7.02-7.04 (6H)

example 3

Synthesis of N,N-bis(biphenyl-4-yl)-N-{6-(9,9-dimethylfluoren-2-yl)biphenyl-3-yl}amine (Compound 1-1)

[0229]The reaction was carried out under the same conditions as those of Example 1, except that phenylboronic acid was replaced with (9,9-dimethylfluoren-2-yl)boronic acid, whereby a white powder of N,N-bis(biphenyl-4-yl)-N-{6-(9,9-dimethylfluoren-2-yl)biphenyl-3-yl}amine (Compound 1-1, 9.0 g, yield: 57%) was obtained.

[0230]The structure of the obtained white powder was identified by NMR.

[0231]1H-NMR (CDCl3) detected 39 hydrogen signals, as follows.

[0232]δ (ppm)=7.56-7.64 (10H), 7.26-50 (18H), 7.02-7.16 (5H), 1.26 (6H)

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Abstract

In the organic electroluminescent device having at least an anode, a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer and a cathode in this order, the hole injection layer includes an arylamine compound of the following general formula (1) and an electron acceptor.In the formula, Ar4 to Ar4 may be the same or different, and represent a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group.

Description

TECHNICAL FIELD[0001]The present invention relates to an organic electroluminescent device which is a preferred self-luminous device for various display devices. Specifically, this invention relates to organic electroluminescent devices (hereinafter referred to as organic EL devices) using specific arylamine compounds doped with an electron acceptor.BACKGROUND ART[0002]The organic EL device is a self-luminous device and has been actively studied for their brighter, superior visibility and the ability to display clearer images in comparison with liquid crystal devices.[0003]In 1987, C. W. Tang and colleagues at Eastman Kodak developed a laminated structure device using materials assigned with different roles, realizing practical applications of an organic EL device with organic materials. These researchers laminated an electron-transporting phosphor and a hole-transporting organic substance, and injected both charges into a phosphor layer to cause emission in order to obtain a high l...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): H01L51/00C07D401/10C07D209/08C07D209/86C07D235/18C07D239/26C07D307/91C07D333/76C07C211/54C07D471/04C07D401/14C07C211/61C07C211/58H01L51/50H01L51/52H10K99/00
CPCH01L51/006C07C211/58C07D401/10C07D209/08C07D209/86C07D235/18C07D239/26C07D307/91C07D333/76H01L51/0072H01L51/0067H01L51/0061H01L51/0059H01L51/0058C07C211/54H01L51/0054H01L51/0052C07D471/04C07D401/14C07C211/61H01L51/0056H01L51/0073H01L51/0074H01L51/5012H01L51/5056H01L51/5072H01L51/5088H01L51/5221H01L51/5206C09B57/008C09B57/00C09B1/00H10K50/00H10K50/17C09K11/06C09K2211/1059H10K85/615H10K85/631H10K85/654H10K50/12H10K50/15H10K50/11H10K50/16H10K85/633H10K85/622H10K85/626H10K85/636H10K85/6572H10K50/81H10K50/82H10K85/624H10K85/6574H10K85/6576
Inventor YOKOYAMA, NORIMASAHAYASHI, SHUICHIYAMAMOTO, TAKESHIKABASAWA, NAOAKIKANDA, DAIZOUMOCHIZUKI, SHUNJICHA, SOON-WOOKPARK, SANG-WOOSONG, JU-MANJEON, KYUNG-SEOK
Owner HODOGOYA CHEMICAL CO LTD
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